Draw the major organic substitution product(s) for (2R,3S)-2-bromo-3-methylpentane reacting with the given nucleophile. İndicate the stereochemistry, including H's, at each stereogenic center. Omit any byproducts. Н Br CH3CH2O (conc.)
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- 1. Which of the following is the strongest nucleophile? Refer to the diagram below with an MeOH, MeSH, etc. 2. Which of the following is true about the stereochemistry of SN1 reaction?a.retention of configuration at the electrophilic centerb.50:50 mixture of retention and inversion of configuration at the electrophilic centerc.inversion of configuration at the electrophilic centerd. slightly more inversion than retention at the electrophilic centerTrue or false? 2-bromo-2-methylpropane undergoes SN1 rather than SN2 because the nucleophile experiences steric hindrance, and a stable carbocation can be formed. When hydroxide ion reacts with 1-chloropropane the main product is 1-propanol.2-Methylpropane have more than one kind of hydrogen and will generate 2 different products with bromination in the presence of uv light. t or f
- Show the SN2 mechanism in the reaction between (S) 2-bromobutane and iodide ion. Label the product and draw a enery diagram for this reaction.Provide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the helpDraw all possible alkenes that could be generated from an E2 elimination reaction of 3-bromo-3-methylhexane. Suggest conditions that can be used to make just one of the alkenes in a controlled manner (i.e., conditions that would lead to formation of just one alkene as the major product).
- Explain the following result. Although alkenes are generally more reactive than alkynes toward electrophiles, the reaction of Cl2 with but-2-yne can be stopped after one equivalent of Cl2 has been added.Consider the E1 reaction of 3-bromo-2-cyclohexyl-butane. How many elimination products are possible? Include (E)/(Z) isomers as separate products.An SN2 mechanism takes place when 3-(bromomethyl)pentane is added to each nucleophile listed below. Which nucleophile will also require an acid-base step after the substitution step in order to produce a neutral (not charged) product? A. LiN(CH3)2 B. NaI C. KN3 D. HSCH3 (Please type answer no write by hend)
- Draw the products and necessary reagents of the three step retrosynthetic reaction sequence shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. Please choose from the following options for each of the reagents. (top reagents options) A. HNO3, cat. H2SO4 B. SO3, cat. H2SO4 C. CH3C(=O)Cl, AlCl3 D. Cl2, FeCl3 E. H2O, HCl (reagents option to the right) (top reagents options) A. HNO3, cat. H2SO4 B. SO3, cat. H2SO4 C. CH3C(=O)Cl, AlCl3 D. Cl2, FeCl3 E. H2O, HClDraw Out Your Predictions of This Reaction: Part A: S-2-chlorohexane + NaOCH3NaOCH3 in methanol. (There are three elimination products and one substitution product.) Part B: 2-chloro-2-methylbutane heated in ethanolDraw the SNl or SN2 reaction with CN for the following molecules t butylchloride , n - butylbromide , 2 -bromobutane . Explain in which mechanism it will react and why ?